The reason for deviation from Mendel's dihybrid cross in T.H. Morgan's experiment is ________.
Linkage
The question asks about the reason why T.H. Morgan's dihybrid crosses showed results that deviated from the expected ratios based on Mendel's principles. Mendel's dihybrid cross experiments led to the principle of independent assortment, predicting a 9:3:3:1 phenotypic ratio in the F2 generation when considering two traits controlled by genes on different chromosomes or far apart on the same chromosome.
T.H. Morgan conducted experiments using the fruit fly, Drosophila melanogaster. He studied the inheritance of several traits, including eye color, body color, and wing size. When performing dihybrid crosses involving certain traits, such as body color (yellow vs. brown) and eye color (white vs. red), Morgan observed that the phenotypic ratios in the F2 generation were significantly different from the expected 9:3:3:1 Mendelian ratio. Instead, he observed a much higher proportion of parental phenotypes and a lower proportion of recombinant phenotypes.
The key concept that explains this deviation is linkage.
Morgan's experiments with Drosophila provided evidence that genes are located on chromosomes and that genes on the same chromosome can be linked. The degree of linkage depends on the distance between the genes on the chromosome. Tightly linked genes show very little recombination, while loosely linked genes show more recombination due to crossing over.
Let's look at why the other options are not the primary reason for the deviation from the Mendelian dihybrid cross ratio observed by Morgan in this specific context:
Therefore, the reason for the deviation from Mendel's dihybrid cross expectations in T.H. Morgan's experiment involving certain linked genes was linkage.
Here's a brief comparison of how independent assortment (Mendel's observation) and linkage affect dihybrid cross results:
| Feature | Mendel's Independent Assortment | Morgan's Linkage |
|---|---|---|
| Gene Location | On different chromosomes OR far apart on the same chromosome. | Close together on the same chromosome. |
| Assortment during Meiosis | Alleles of different genes assort independently. | Alleles of linked genes tend to be inherited together. |
| Gamete Types | Four types of gametes produced in equal proportions (if parents are heterozygous). | Parental type gametes produced in higher proportion than recombinant type gametes. |
| F2 Phenotypic Ratio (starting from heterozygous parents for both traits) | Typically 9:3:3:1 (for complete dominance). | Deviates from 9:3:3:1, with higher proportion of parental phenotypes. |
| Term | Definition | Relevance to Question |
|---|---|---|
| Mendel's Dihybrid Cross | Studying inheritance of two traits simultaneously; predicts independent assortment if genes are unlinked. | Provides the expected baseline (9:3:3:1 ratio) that Morgan observed deviation from. |
| Independent Assortment | Alleles of different genes separate independently during gamete formation. | Mendel's principle, contradicted by linked genes. |
| Linkage | Genes on the same chromosome inherited together. | The direct reason for deviation from Mendelian ratios in Morgan's experiments. |
| T.H. Morgan | Geneticist who used Drosophila; discovered sex-linkage and gene linkage. | His experiments provided crucial evidence for linkage. |
The concept of linkage discovered by Morgan was a major advancement in genetics. It showed that inheritance patterns are not always as simple as predicted by independent assortment, especially when genes reside on the same chromosome. The closer two genes are on a chromosome, the stronger the linkage and the less likely they are to be separated by crossing over during meiosis. This allowed Morgan and his students to map the relative positions of genes on chromosomes based on the frequency of recombination (crossing over) between them.
Crossing over, also known as recombination, is an event during meiosis where homologous chromosomes exchange segments. This exchange can separate alleles of linked genes, leading to recombinant gametes. The frequency of crossing over between two linked genes is roughly proportional to the distance between them. This forms the basis of genetic mapping.
Given below are two statements:
Statement I: Phenylketonuria is an example of Pleiotropy
Statement II: Affected individuals lack an enzyme which converts phenylalanine into tyrosine
In the light of the above statements, choose the most appropriate answer from the options given below:
Individuals with karyotype of 44+XXY having overall masculine development with few feminine development like Gynaecomastia has ________ chromosomal disorder.
Sutton united the knowledge of chromosomal segregation with Mendelian principles and called it the _______.